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首页> 外文期刊>Archivum Immunologiae et Therapiae Experimentalis >Experimental anti-GBM nephritis as an analytical tool for studying spontaneous lupus nephritis
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Experimental anti-GBM nephritis as an analytical tool for studying spontaneous lupus nephritis

机译:实验性抗GBM肾炎作为研究自发性狼疮肾炎的分析工具

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摘要

Systemic lupus erythematosus (SLE) is an autoimmune disease that results in immune-mediated damage to multiple organs. Among these, kidney involvement is the most common and fatal. Spontaneous lupus nephritis (SLN) in mouse models has provided valuable insights into the underlying mechanisms of human lupus nephritis. However, SLN in mouse models takes 6–12 months to manifest; hence there is clearly the need for a mouse model that can be used to unveil the pathogenic processes that lead to immune nephritis over a shorter time frame. In this article more than 25 different molecules are reviewed that have been studied both in the anti-glomerular basement membrane (anti-GBM) model and in SLN and it was found that these molecules influence both diseases in a parallel fashion, suggesting that the two disease settings share common molecular mechanisms. Based on these observations, the authors believe the experimental anti-GBM disease model might be one of the best tools currently available for uncovering the downstream molecular mechanisms leading to SLN. Keywords: autoantibodies - mouse models - SLE - therapy - glomerular disease
机译:系统性红斑狼疮(SLE)是一种自身免疫性疾病,可导致免疫介导的多个器官受损。其中,肾脏受累是最常见和致命的。小鼠模型中的自发性狼疮性肾炎(SLN)为了解人类狼疮性肾炎的潜在机制提供了宝贵的见识。但是,小鼠模型中的SLN需要6到12个月的时间才能显现出来。因此,显然需要一种可用于揭示在较短时间内导致免疫性肾炎的致病过程的小鼠模型。本文回顾了在抗肾小球基底膜(anti-GBM)模型和SLN中研究的超过25种不同分子,发现这些分子以平行的方式影响两种疾病,这表明这两种疾病背景共有共同的分子机制。基于这些观察,作者认为,实验性抗GBM疾病模型可能是目前可用于发现导致SLN的下游分子机制的最佳工具之一。关键词:自身抗体-小鼠模型-SLE-治疗-肾小球疾病

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